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b-ONE MOBIO Total Knee System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213673
510(k) Type
Traditional
Applicant
b-ONE ORTHO, Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/21/2022
Days to Decision
60 days
Submission Type
Summary

b-ONE MOBIO Total Knee System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213673
510(k) Type
Traditional
Applicant
b-ONE ORTHO, Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/21/2022
Days to Decision
60 days
Submission Type
Summary